DRKS00015272尚未招募未知
Randomized, patient- and observer-blinded evaluation of P6 stimulation for the prevention of nausea and vomiting in the postoperative period in patients receiving routine pharmacological prophylaxis. - P6NV
Klinik für Anästhesie und Intensivtherapie, Philipps-Universität Marburg0 个研究点目标入组 3,500 人开始时间: 2018年8月15日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
- 入组人数
- 3,500
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized controlled study
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 one（—）
- 性别
- All
入选标准
- •Patients undergoing scheduled surgery for general anesthesia.
- •- Patients 18 years and older
- •- Patients are able to consent
- •- sufficient command of the German language to be able to carry out a medical anamnesis and a postoperative survey without a translator
- •- Patients agree to undergo P6 acupressure / P6 acupuncture
- •- Patients have a PONV risk, which requires one or more of the following pharmacological intervention (s) against PONV at the treating clinic according to the instructions given there or in the opinion of the attending anesthesiologist.
- •-- Application of 4-8 mg dexamethasone
- •-- Application of 4-8 mg ondansetron
- •-- Application of 1 mg granisetron
- •-- Administration of 0.5-1.5 mg droperidol
- •-- Application of 0.5-1.5 mg haloperidol
- •-- Application of 50-70 mg dimenhydrinate
- •-- TIVA (instead of anesthesia maintenance with a volatile anesthetic)
排除标准
- •- Rejection of study participation by patients
- •- Patient already participated in study
- •- patients undergoing chemotherapy or antineoplastic therapy / radiotherapy within the last 4 weeks
- •- Regional anesthetic procedure as the sole anesthesia procedure
- •- Pregnancy and breast feeding period
- •- Foreseeable requirement of postoperative post-ventilation / intensive care
- •- Dementia
- •- Preoperative nausea
研究者
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